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Carnitine palmitoyltransferase 2 (CPT2) deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods without food (fasting). There are three main types of CPT2 deficiency: a lethal neonatal form, a severe infantile hepatocardiomuscular form, and a myopathic form. The neonatal and infantile forms are severe multisystemic diseases characterized ...
Is the diet difficult to do/expensive? CPT II deficiency is primarily treated by a high carbohydrate and fat modified/decreased diet that is given at regular defined intervals around the clock or even, in some cases, during the initial period by continuous nasogastric feeding As the diet is essentially normal it should not be a financial burden.
Diet: CPT2 deficiency is a fat metabolism disorder. As such diet is extremely important in order to avoid disease symptoms. Usually a low fat, high carbohydrate food plan is recommended. Carbohydrates provide several types of sugars to the body and can be used as a source of energy. Sometimes, eating sugar during an episodic attack of symptoms can provide relief.
We had never considered how diet affected his muscles, but thought that exercise was the main trigger. Looking into diet suggestions for people with CPT2 deficiency, I'm seeing suggestions for low fat/high carbohydrate diets, since they get most of their energy from sugars.
I am one of the very few people to have been diagnosed with a genetic disorder called Carnitine palmitoyltransferase II Deficiency, or "CPT2 Deficiency". In between episodes, life with CPT2 is very normal. However, during an episode CPT2 patients experience muscle pain, rhabdomyolysis, myoglobinuria and other unpleasant symptoms.
3. Take the right diet, go for low fat and high carbohydrate. As mentioned elsewhere on this website, a diet high in fatty acids can provoke an attack in CPT 2 deficient patients, as the metabolism cannot cope with the necessary amounts required by the muscle cells.